Nadine Schliecker Email

Nadine Schliecker Email

Head of Regulatory Affairs and Pharmacovigilance, QPPV and Stufenplanbeauftragte, Informationsbeauftragte @ Aqvida GmbH

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Nadine Schliecker's Location

Hamburg, Hamburg, Germany

Nadine Schliecker's Work

  • Head of Regulatory Affairs and Pharmacovigilance, QPPV and Stufenplanbeauftragte, Informationsbeauftragte @ Aqvida GmbH
  • Head of Drug Regulatory Affairs and Licensing @ medac GmbH
  • Project Manager Drug Regulatory Affairs and European Union @ medac GmbH
  • Project Manager Drug Regulatory Affairs and Pharmaceutical Development @ medac GmbH
  • Manager Regulatory Affairs, Betäubungsmittelbeauftragte @ Essex Pharma GmbH
  • Project Manager Regulatory Affairs and Pharmaceutical Development @ Tiefenbacher Group
  • Pharmaziepraktikantin @ Fleming Apotheke
  • Pharmaziepraktikantin @ Schering AG

Nadine Schliecker's Education

  • The University of Bonn

    Masters

    2001 - 2003
  • University of Hamburg

    1996 - 2000

Nadine Schliecker's Summary

Nadine Schliecker, based in Hamburg, Hamburg, Germany, is currently a Head of Regulatory Affairs and Pharmacovigilance, QPPV and Stufenplanbeauftragte, Informationsbeauftragte at Aqvida GMBH, bringing experience from previous roles at Medac GMBH and Essex Pharma GMBH. Nadine Schliecker holds a 2001 - 2003 Masters @ The University of Bonn.

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